NZ513482A

NZ513482A - T helper cell epitodes derived from canine distemper virus for producing an immune response in an animal

Info

Publication number: NZ513482A
Application number: NZ513482A
Authority: NZ
Inventors: David Charles Jackson; Souravi Ghosh; John Walker
Original assignee: Univ Melbourne; Csl Ltd; Commw Scient Ind Res Org; Queensland Inst Med Res; Inst Medical W & E Hall
Priority date: 1999-02-05
Filing date: 2000-02-07
Publication date: 2003-08-29
Also published as: CA2361658C; EP1147212A4; ES2332701T3; US20060199177A1; ZA200106413B; CY1109710T1; DE60042816D1; EP1147212B1; EP1147212A1; JP2011121965A; EP2103691A1; US20070248615A1; AU765164B2; KR100955668B1; US20050037014A1; ATE440960T1; US7097844B2; KR100905264B1; AU2783600A; DK1147212T3

Abstract

Compositions comprising T helper cell epitopes derived from Canine Distemper Virus (CDV) are described, along with the use of said compositions for raising an immune response in an animal. Also detailed are further compositions which additionally contain at least one B cell epitope.

Description

<div class="application article clearfix" id="description"> WO 00/46390 PCT/AUOQ/00070 1 T Helper cell epitopes FIELD OF THE INVENTION 5 The present invention relates to T helper cell epitopes derived from Canine Distemper Virus (CDV). The present invention relates to compositions including at least one T helper cell epitope and optionally B cell epitopes and/or CTL epitopes. 10 BACKGROUND OF THE INVENTION For any peptide to be able to induce an effective antibody response it must contain particular sequences of amino acids known as epitopes that are recognised by the immune system. In particular, for antibody responses, 15 epitopes need to be recognised by specific immunoglobulin (Ig) receptors present on the surface of B lymphocytes. It is these cells which ultimately differentiate into plasma cells capable of producing antibody specific for that epitope. In addition to these B cell epitopes, the immunogen must also contain epitopes that are presented by antigen presenting cells (APC) to 20 specific receptors present on helper T lymphocytes, the cells which are necessary to provide the signals required for the B cells to differentiate into antibody producing cells. In the case of viral infections and in many cases of cancer, antibody is of limited benefit in recovery and the immune system responds with cytotoxic 25 T cells (CTL) which are able to kill the virus-infected or cancer cell. Like helper T cells, CTL are first activated by interaction with APC bearing their specific peptide epitope presented on the surface, this time in association with MHC class I rather than class II molecules. Once activated the CTL can engage a target cell bearing the same peptide/class I complex and cause its lysis. It is 30 also becoming apparent that helper T cells play a role in this process; before the APC is capable of activating the CTL it must first receive signals from the helper T cell to upregulate the expression of the necessary costimulatory molecules. Helper T cell epitopes are bound by molecules present on the surface 35 of APCs that are coded by class II genes of the major histocompatibility complex (MHC). The complex of the class II molecule and peptide epitope is WO 00/46390 PCT/AUOO/00070 then recognised by specific T-cell receptors (TCR) on the surface of T helper lymphocytes. In this way the T cell, presented with an antigenic epitope in the context of an MHC molecule, can be activated and provide the necessary signals for the B lymphocyte to differentiate. Traditionally the source of 5 helper T cell epitopes for a peptide immunogen is a carrier protein to which peptides are covalently coupled but this coupling procedure can introduce other problems such as modification of the antigenic determinant during the coupling process and the induction of antibodies against the carrier at the expense of antibodies which are directed toward the peptide (Schutze, M. P., 10 Leclerc, C. Jolivet, M. Audibert, F. Chedid, L. Carrier-induced epitopic suppression, a major issue for future synthetic vaccines. J Immunol. 1985,135, 2319-2322; Dijohn, D., Torrese, J. R. Murillo, J. Herrington, D.A. et al. Effect of priming with carrier on response to conjugate vaccine. The Lancet. 1989, 2, 1415-1416). Furthermore, the use of irrelevant proteins in the preparation 15 introduces issues of quality control. The choice of appropriate carrier proteins is very important in designing peptide vaccines and their selection is limited by factors such as toxicity and feasibility of their large scale production. There are other limitations to this approach including the size of the peptide load that can be coupled and the dose of carrier that can be safely administered 20 (Audibert, F. a. C., L. 1984. Modern approaches to vaccines. Molecular and chemical basis of virus virulence and immunogenicity., Cold Spring Harbor Laboratory, New York.). Although carrier molecules allow the induction of a strong immune response they are also associated with undesirable effects such as suppression of the anti-peptide antibody response (Herzenberg, L. A. and 25 Tokuhisa, T. 1980. Carrier-priming leads to hapten-specific suppression. Nature 285:664; Schutze, M. P., Leclerc, C., Jolivet, M., Audibert, F., and Chedid, L. 1985. Carrier-induced epitopic suppression, a major issue for future synthetic vaccines. J Immunol 135:2319; Etlinger, H. M., Felix, A. M., Gillessen, D., Heimer, E. P., Just, M., Pink, J. R., Sinigaglia, F., Sturchler, D., 30 Takacs, B., Trzeciak, A., and et, a. 1988. Assessment in humans of a synthetic peptide-based vaccine against the sporozoite stage of the human malaria parasite, Plasmodium falciparum. J Immunol 140:626). In general then, an immunogen must contain epitopes capable of being recognised by helper T cells in addition to the epitopes that will be recognised 35 by surface Ig or by the receptors present on cytotoxic T cells. It should be realised that these types of epitopes may be very different. For B cell epitopes, WO 00/46390 PCT/AU00/00070 3 conformation is important as the B cell receptor binds directly to the native immunogen. In contrast, epitopes recognised by T cells are not dependent on conformational integrity of the epitope and consist of short sequences of approximately nine amino acids for CTL and slightly longer sequences, with 5 less restriction on length, for helper T cells. The only requirements for these epitopes are that they can be accommodated in the binding cleft of the class I or class II molecule respectively and that the complex is then able to engage the T-cell receptor. The class II molecule's binding site is open at both ends allowing a much greater variation in the length of the peptides bound (Brown, 10 J. H., T. S. Jardetzky, J. C. Gorga, L. J. Stern, R. G. Urban, J. L. Strominger and D. C. Wiley. 1993. Three-dimensional structure of the human class II histocompatibility antigen HLA-DRl. Nature 364:33) with epitopes as short as 8 amino acid residues being reported (Fahrer, A.M., Geysen, H.M., White, D.O., Jackson, D.C. and Brown,L.E. Analysis of the requirements for class 15 II-restricted T-cell recognition of a single determinant reveals considerable diversity in the T-cell response and degeneracy of peptide binding to I-Ed J. Immunol. 1995. 155: 2849-2857). Canine distemper virus (CDV) belongs to the subgroup of morbillivirus of paramyxovirus family of negative-stranded RNA viruses. Other viruses 20 which are members of this group are measles virus and rinderpest virus, Development of peptide based vaccines has aroused considerable interest in identification of B and T cell epitopes from sequences of proteins. The rationale for using T cell epitopes from proteins such as the F protein of CDV is that young dogs are inoculated against CDV in early life and will therefore 25 possess helper T cells specific for helper T cell epitopes present on this protein. Subsequent exposure to a vaccine which contains one or more of the epitopes will therefore result in recruitment of existing helper T cells and consequently an enhanced immune response. Such helper T cell epitopes could, however, be administered to unprimed animals and still induce an 30 immune response. The present inventors aimed to identify canine T cell epitopes from the sequence of CDV fusion protein so that these epitopes can then be used in the design of peptide based vaccines, in particular, for the canine and related species. LHRH (Luteinising hormone releasing hormone) is a ten amino acids 35 long peptide hormone whose sequence is conserved in mammals. It is secreted by the hypothalamus and controls the reproductive physiology of both WO 00/46390 PCT/AUOO/00070 4 males and females. The principle of development of LHRH- based immunocontraceptive vaccines is based on observations that antibodies to LHRH block the action of the hormone on pituitary secretion of luteinising hormone and follicle stimulating hormone, leading to gonadal atrophy and 5 sterility in mammals. Most LHRH vaccines that have been developed consist of LHRH chemically conjugated to protein carriers to provide T cell help for the generation of anti-LHRH antibodies. It has been shown that upon repeated inoculation of LHRH-protein carrier conjugates the anti-LHRH titre decreases 10 due to the phenomenon known as "carrier induced epitope suppression". One aim of the present inventors is to replace protein carriers in the vaccines with defined T helper epitopes (TH-epitopes) so as to eliminate "carrier induced epitope suppression". 15 SUMMARY OF THE INVENTION The present inventors have identified a number of 17 residue peptides each of which includes a T helper cell epitope. As will be readily appreciated the majority of these peptides are not minimal T helper cell epitopes. 20 Typically class II molecules have been shown to be associated with peptides as short as 8 amino acids (Fahrer et al., 1995 ibid) but usually of 12-19 amino acids (Chicz, R. M., Urban, R. G., Gorga, J. C., Vignali, D. A. A., Lane, W. S. and Strominger, }. L. Specificity and promiscuity among naturally processed peptides bound to HLA-DR alleles. J Exp Med 1993, 178, 27-47; Chicz, R. M., 25 Urban, R. G., Lane, W. S., Gorga, J. C., Stern, L. J., Vignali, D. A. A. and Strominger, J. L. Predominant naturally processed peptides bound to HLA-DRl are derived from MHC-related molecules and are heterogeneous in size. Nature 1992, 358, 764-8), although, peptides up to 25 amino acids in length have been reported to bind to class II (reviewed in Rammensee, H.-G. Chemistry of 30 peptide associated with class I and class II molecules. Curr Opin Immunol 1995, 7, 85-95.). Thus peptide epitopes that range in length between 8 and 25 amino acid residues can bind to class II molecules. The shorter peptides are "core" epitopes that may have less activity than longer sequences but it is a trivial 35 exercise to truncate longer sequences at the N- or the C-terminus to yield WO 00/46390 PCT/AU00/00070 5 shorter sequences that have the same or better activity than the parent sequence. Accordingly in a first aspect the present invention consists in a T helper cell epitope, the epitope being contained within a peptide sequence selected from the group consisting of SSKTQTHTQQDRPPQPS; QPSTELEETRTSRARHS; RHSTTSAQRSTHYDPRT; PRTSDRPVSYTMNRTRS; TRSRKQTSHRLKNIPVH; SHQYLVIKLIPNASLIE; IGTDNVHYKIMTRPSHQ; YKIMTRPSHQYLVIKLI; KLIPNASLIENCTKAEL; AELGEYEKLLNSVLEPI; KLLNSVLEPINQALTLM; EPINQALTLMTKNVKPL; FAGWLAGVALGVATAA; GVALGVATAAQITAGIA; TAAQITAGIALHQSNLN; GLALHQSNLNAQAIQSL; NLNAQAIQSLRTSLEQS; QSLRTSLEQSNKAIEEI; EQSNKAIEEIREATQET; TELLSIFGPSLRDPISA; PRYIATNGYLISNFDES; CIRGDTSSCARTLVSGT; DESSCVFVSESAICSQN; TSTIINQSPDKLLTFIA, SPDKLLTFIASDTCPLV and SGRRQRRFAGWLAGVA. In a second aspect the present invention consists in a composition for use in raising an immune response in an animal, the composition comprising at least one T helper cell epitope, the at least one T helper cell epitope being contained within a peptide sequence selected from the group consisting of SSKTQTHTQQDRPPQPS; QPSTELEETRTSRARHS; RHSTTSAQRSTHYDPRT; PRTSDRPVSYTMNRTRS; TRSRKQTSHRLKNIPVH; SHQYLVIKLIPNASLIE; IGTDNVHYKIMTRPSHQ; YKIMTRPSHQYLVIKLI; KLIPNASLIENCTKAEL; AELGEYEKLLNSVLEPI; KLLNSVLEPINQALTLM; EPINQALTLMTKNVKPL; FAGWLAGVALGVATAA; GVALGVATAAQITAGIA; TAAQITAGIALHQSNLN; GLALHQSNLNAQAIQSL; NLNAQAIQSLRTSLEQS; QSLRTSLEQSNKAIEEI; EQSNKAIEEIREATQET; TELLSIFGPSLRDPISA; PRYIATNGYLISNFDES; CIRGDTSSCARTLVSGT; DESSCVFVSESAICSQN; TSTIINQSPDKLLTFIA, SPDKLLTFIASDTCPLV and SGRRQRRFAGWLAGVA. In a preferred embodiment of the present invention the composition comprises at least one peptide selected from the group consisting of SSKTQTHTQQDRPPQPS; QPSTELEETRTSRARHS; RHSTTSAQRSTHYDPRT; PRTSDRPVSYTMNRTRS; TRSRKQTSHRLKNIPVH; SHQYLVIKLIPNASLIE; IGTDNVHYKIMTRPSHQ; YKIMTRPSHQYLVIKLI; KLIPNASLIENCTKAEL; AELGEYEKLLNSVLEPI; KLLNSVLEPINQALTLM; EPINQALTLMTKNVKPL; FAGWLAGVALGVATAA; GVALGVATAAQITAGIA; TAAQITAGIALHQSNLN; GLALHQSNLNAQAIQSL; NLNAQAIQSLRTSLEQS; QSLRTSLEQSNKAIEEI; EQSNKAIEEIREATQET; TELLSIFGPSLRDPISA; PRYIATNGYLISNFDES; WO 00/46390 PCT/AUOO/00070 6 CIRGDTSSCARTLVSGT; DESSCVFVSESAICSQN; TSTIINQSPDKLLTFIA, SPDKLLTFIASDTCPLV and SGRRQRRFAGWLAGVA. It is further preferred that the composition further comprises at least one B cell epitope and/or at least one CTL epitope. In yet another preferred embodiment the at least one B cell epitope and/or the at least one CTL epitope are linked to at least one of the T helper cell epitopes. It is also preferred that the composition comprises a plurality of epitope constructs in which each comprises at least one T helper cell epitope and at least one B cell epitope. Alternatively the composition may comprises a plurality of epitope constructs in which each comprises at least one T helper cell epitope and at least one CTL epitope. It will be understood that the B cell epitope or CTL epitope may be any epitope. A currently preferred B cell epitope is an LHRH B cell epitope. The composition of the present invention may comprises a plurality of T helper cell epitopes. These epitopes may be singular or be linked together to form a single polypeptide. It will be understood that where the epitopes are linked to together in a single polypeptide the epitopes may be contiguous or spaced apart by additional amino acids which are not themselves part of the T helper cell epitopes. As discussed above in one embodiment the T helper cell epitopes and at least one B cell epitope and/or at least one CTL epitope in which the epitopes are linked. This may be done by simple covalent linkage of the peptides. In another embodiment the epitopes are polymerised, most preferably such as described in PCT/AU98/00076, the disclosure of which is incorporated herein by reference. In yet another preferred embodiment the composition further comprises a pharmaceutical^ acceptable excipient, preferably an adjuvant. In a further aspect the present invention consists in a method of inducing an immune response in an animal, the method comprising administering to the animal the composition of the second aspect of the present invention. Pharmaceutically acceptable carriers or diluents include those used in compositions suitable for oral, rectal, nasal, topical (including buccal and sublingual), vaginal, parenteral (including subcutaneous, intramuscular, intravenous, intradermal, intrathecal and epidural) administration. They are non-toxic to recipients at the dosages and concentrations employed. WO 00/46390 PCT/AUOO/00070 Representative examples of pharmaceutical^ acceptable carriers or diluents include, but are not limited to water, isotonic solutions which are preferably buffered at a physiological pH (such as phosphate-buffered saline or Tris-buffered saline) and can also contain one or more of, mannitol, lactose, 5 trehalose, dextrose, glycerol, ethanol or polypeptides (such as human serum albumin). The compositions may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art of pharmacy. As mentioned it is preferred that the composition includes an 10 adjuvant. As will be understood an "adjuvant" means a composition comprised of one or more substances that enhances the immunogenicity and efficacy of a vaccine composition. Non-limiting examples of suitable adjuvants include squalane and squalene (or other oils of animal origin); block copolymers; detergents such as Tween®-80; Quil® A, mineral oils such as Drakeol or 15 Marcol, vegetable oils such as peanut oil; Corynebacterium-derived adjuvants such as Corynebacterium parvum; Propionibacterium-deTived adjuvants such as Propionibacterium acne; Mycobacterium bovis (Bacille Calmette and Guerin or BCG); interleukins such as interleukin 2 and interleukin 12; monokines such as interleukin 1; tumour necrosis factor; interferons such as gamma interferon; 20 combinations such as saponin-aluminium hydroxide or Quil-A aluminium hydroxide; liposomes; ISCOM adjuvant; mycobacterial cell wall extract; synthetic glycopeptides such as muramyl dipeptides or other derivatives; Avridine; Lipid A derivatives; dextran sulfate; DEAE-Dextran or with aluminium phosphate; carboxypolymethylene such as Carbopol' EMA; acrylic 25 copolymer emulsions such as Neocryl A640 (e.g. U.S. Pat. No. 5,047,238); vaccinia or animal poxvirus proteins; sub-viral particle adjuvants such as cholera toxin, or mixtures thereof. As will be recognised by those skilled in the art modifications may be made to the peptides of the present invention without complete abrogation of 30 biological activity. These modifications include additions, deletions and substitutions, in particular conservative substitutions. It is intended that peptides including such modifications which do not result in complete loss of activity as T helper cell epitopes are within the scope of the present invention. WO 00/46390 PCT/AU00/00070 8 Whilst the concept of substitution is well known in the field the types of substitutions envisaged are set out below. Original Residue Exemplary Substitutions Preferred Substitutions Ala (A) val; leu; ile val Arg (R) lys; gin; asn lys Asn (N) gin; his; lys; arg gin Asp (D) glu glu Cys (C) ser ser Gin (Q) asn asn Glu (El asp asp Gly (G) pro pro His (HI asn; gin; lys; arg arg Ile (I) leu; val; met; ala; phe norleucine leu Leu (L) norleucine, ile; val; met; ala; phe ile Lvs (K) arg; gin; asn arg Met (M) leu; phe; ile; leu Phe (F) leu; val; ile; ala leu Pro (P) Rly sly Ser(S) thr thr Thr (T ser ser Trp (W) tyr tyr Tyr (Y) trp; phe; thr; ser phe Val (V) ile; leu; met; phe ala; norleucine leu Another type of modification of the peptides envisaged include, but are not limited to, modifications to side chains, incorporation of unnatural amino acids and/or their derivatives during peptide synthesis and the use of crosslinkers and other methods which impose conformational constraints on the peptides. WO 00/46390 PCT/AUOO/00070 9 Examples of side chain modifications contemplated by the present invention include, but are not limited to, modifications of amino groups such as by reductive alkylation by reaction with an aldehyde followed by reduction with NaBH4; amidation with methylacetimidate; acylation with 5 acetic anhydride; carbamoylation of amino groups with cyanate; trinitrobenzylation of amino groups with 2,4,6-trinitrobenzene sulphonic acid (TNBS); acylation of amino groups with succinic anhydride and tetrahydrophthalic anhydride; and pyridoxylation of lysine with pyridoxal-5'-phosphate followed by reduction with NaBH,. 10 The guanidine group of arginine residues may be modified by the formation of heterocyclic condensation products with reagents such as 2,3-butanedione, phenylglyoxal and glyoxal. The carboxyl group may be modified by carbodiimide activation via O-acylisourea formation followed by subsequent derivitisation, for example, 15 to a corresponding amide. Tryptophan residues may be modified by, for example, oxidation with N-bromosuccinimide or alkylation of the indole ring with 2-hydroxy-5-nitrobenzyl bromide or sulphenyl halides. Tyrosine residues on the other hand, may be altered by nitration with tetranitromethane to 20 form 3-nitrotyrosine derivative. Modification of the imidazole ring of a histidine residue may be accomplished by alkylation with iodoacetic acid derivatives or N-carbethoxylation with diethylpyrocarbonate. Examples of incorporating unnatural amino acids and derivatives 25 during peptide synthesis include, but are not limited to, use of norleucine, 4-amino butyric acid, 4-amino-3-hydroxy-5-phenylpentanoic acid, 6-aminohexanoic acid, t-butylglycine, norvaline, phenylglycine, ornithine, sarcosine, 4-amino-3-hydroxy-6-methylheptanoic acid; 2-thienyl alanine and/or D-isomers of amino acids. 30 The peptides of the present invention may be derived from CDV. Alternatively, the peptide or combination of peptide epitopes may be produced by recombinant DNA technology. It is, however, preferred that the peptides are produced synthetically using methods well known in the field. For example, the peptides may be synthesised using solution synthesis or solid 35 phase synthesis as described, for example, in Chapter 9 entitled "Peptide Synthesis" by Atherton and Sheppard which is included in a publication WO 00/46390 PCT/AU00/00070 10 entitled "Synthetic Vaccines" edited by Nicholson and published by Blackwell Scientific Publications. Preferably a solid phase support is utilised which may be polystyrene gel beads wherein the polystyrene may be cross-linked with a small proportion of divinylbenzene (e.g. 1%) which is further swollen by 5 lipophilic solvents such as dichloromethane or more polar solvents such as dimethylformamide (DMF). The polystyrene maybe functionalised with chloromethyl or aminomethyl groups. Alternatively, cross-linked and functionalised polydimethyl-acrylamide gel is used which may be highly solvated and swollen by DMF and other dipolar aprotic solvents. Other 10 supports can be utilised based on polyethylene glycol which is usually grafted or otherwise attached to the surface of inert polystyrene beads. In a preferred form, use may be made of commercial solid supports or resins which are selected from PAL-PEG-PS, PAC-PEG-PS, KA, KR or TGR. In solid state synthesis, use is made of reversible blocking groups 15 which have the dual function of masking unwanted reactivity in the a-amino, carboxy or side chain functional groups and of destroying the dipolar character of amino acids and peptides which render them inactive. Such functional groups can be selected from t-butyl esters of the structure RCO-OCMe3-CO. Use may also be made of the corresponding benzyl esters having the structure 20 RCO-OCH2-C8H5 and urethanes having the structure CeH5CH2OCO-NHR which are known as the benzyloxycarbonyl or Z-derivatives and any Me3-COCO-NHR, which are known as t-butoxyl carbonyl, or Boc derivatives. Use may also be made of derivatives of fluorenyl methanol and especially the fluorenyl-methoxy carbonyl or Fmoc group. Each of these types of protecting 25 group is capable of independent cleavage in the presence of one other so that frequent use is made, for example, of BOC-benzyl and Fmoc-tertiary butyl protection strategies. Reference also should be made to a condensing agent to link the amino and carboxy groups of protected amino acids or peptides. This may be done by 30 activating the carboxy group so that it reacts spontaneously with a free primary or secondary amine. Activated esters such as those derived from p-nitrophenol and pentafluorophenol may be used for this purpose. Their reactivity may be increased by addition of catalysts such as 1-hydroxybenzotriazole. Esters of triazine DHBT (as discussed on page 215-216 of the abovementioned 35 Nicholson reference) also may be used. Other acylating species are formed in situ by treatment of the carboxylic acid (i.e. the N-alpha-protected amino acid WO 00/46390 PCT/AU0O/OOO7O 11 or peptide) with a condensing reagent and are reacted immediately with the amino component (the carboxy or C-protected amino acid or peptide). Dicyclohexylcarbodiimide, the BOP reagent (referred to on page 216 of the Nicholson reference), O'Benzotriazole-N, N, NW-tetra methyl-uronium 5 hexafluorophosphate (HBTU) and its analogous tetrafluoroborate are frequently used condensing agents. The attachment of the first amino acid to the solid phase support may be carried out using BOC-amino acids in any suitable manner. In one method BOC amino acids are attached to chloromethyl resin by warming the triethyl 10 ammonium salts with the resin. Fmoc-amino acids may be coupled to the p-alkoxybenzyl alcohol resin in similar manner. Alternatively, use may be made of various linkage agents or "handles" to join the first amino acid to the resin. In this regard, p-hydroxymethyl phenylacetic acid linked to aminomethyl polystyrene may be used for this purpose. 15 Throughout this specification the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps. 20 DETAILED DESCRIPTION OF THE INVENTION In order that the nature of the present invention may be more readily understood preferred forms there of will now be described with reference to 25 the following non-limiting examples. FIGURE LEGENDS Figure 1. Amino acid sequence of the fusion protein of CDV 30 Figure 2. Stimulation indices to Th-epitope P25 and its truncated versions from dogs immunised with P25-LHRH. (X-axis concentration of peptides nmoles/well) Figure 3. Stimulation indices to Th-epitope P27 and its truncated 15-mer from dogs immunised with P27-LHRH. (X-axis concentration of 35 peptides nmoles/well) WO 00/46390 PCT/AUOO/00070 12 Figure 4. Stimulation indices to Th-epitope P35 and its truncated versions from dogs immunised with P35-LHRH. (X-axis concentration of peptides nmoles/well) 5 EXAMPLE 1 Identification of Thelper cell epitopes Methods and Results: 10 Towards identification of canine T cell epitopes 94, 17 residue overlapping peptides were designed encompassing the entire sequence of fusion protein of canine distemper virus (CDV). The 17mer peptides were numbered sequentially for identification starting from the N-terminus. The sequence of the fusion protein of CDV as determined by Barrett et al 1987 15 (Virus Res. 8, 373-386) is shown in Figure 1. The peptides were used in T-cell proliferation assays using peripheral blood lymphocytes (PBMC) from dogs immunised with Canvac™ 3 in 1 vaccine (CSL Limited) which contains live CDV. Initially, four dogs were used and they were boosted with the Canvac™ 20 3 in 1 vaccine twice with four to six weeks between each vaccination. The dogs were bled after each booster vaccination and the PBMCs were tested against the peptides. No significant proliferation to peptides was observed. Since CDV has been reported to be lymphotropic and the vaccine consists of live CDV, there was the possibility that it may be sequestered in 25 lymphoid organs preventing significant numbers of precursor T cells entering the peripheral system. To increase the frequency of peripheral blood anti-CDV T cells dogs were boosted with heat killed CDV (obtained as a pellet from virus culture medium, CSL Limited). Two weeks later, the dogs were bled and the PBMCs tested for proliferation against the peptides. Again there was no 30 proliferation to the peptide antigens. An alternate strategy was used to increase the precursor frequency of specific T cells recognising the CDV peptides. Fresh PBMCs obtained from these hyperimmunised dogs were subjected to stimulations vitro with pools of all 94 peptides for 30 minutes at 37°C. The cells were then washed to 35 remove any excess peptides and cultured for 7 days. This population of Tcells was then tested with autologous APCs with evexy single peptide as the antigen. WO 00/46390 PCT/AU00/00070 13 Table 1 shows the peptides to which significant (stimulation index >2) levels of proliferation were observed. To confirm this observation, the same four dogs were bled again, five weeks after receiving the dose of killed virus. The PBMCs were stimulated in 5 vitro with pools of either all 94 peptides or peptides 21-40 (because most of the activity was in this region) and after 7 days of culture the stimulated T cells were tested against individual peptides. Significant stimulatory indices were obtained with all peptides, confirming the above results. Four more dogs which received only one dose of 3 in 1 vaccine were tested using the in vitro 10 stimulation method and all four dogs responded to the majority of peptides shown in Table 2. The above peptides were also tested on cells from additional dogs, with results shown in Table 3. Peptides P64, P74 and P75 were also shown to react strongly with peripheral blood mononuclear cells from dogs of various breeds 15 immunised with CDV (Table 4), and are therefore identified as strong T-helper epitopes. Table 1. Identification of canine T cell epitopes from the sequence of fusion protein of CDV. 20 Peptides Beagle Foxhound (DoS#18) Beagle Foxhound (Dog#19) Beagle Foxhound (DOR#20) Beagle Foxhound (Dos#21) P2 2* <2 8 3.9 P4 4.9 <2 3.3 4.6 P6 2.5 <2 4 5.1 plO 2.3 <2 3.2 9.1 p24 5.8 9.9 2.8 29 p25 3.2 11.9 4.5 17 p27 3.3 34 6.7 14.8 p29 3.5 42 4.4 <2 P35 3.1 57 3.3 22 P36 6.7 3.7 3.3 16 p37 6.9 10.9 8.2 26 p38 2.8 6.7 3.6 4.2 p47 3.3 85.7 2.9 1.9 p62 <2 51 5.6 4.2 p68 6.6 <2 <2 11.7 * Stimulatory index WO 00/46390 PCT/AU00/00070 14 Table 2. Identification of canine T cell epitopes from the sequence of fusion protein of CDV. Peptides Beagle Foxhound (Dog #70) Beagle Foxhound (Dor #71) Beagle Foxhound (Dog #72) Beagle Foxhound (Dog #73) P8 2.2 p22 2.6 p24 3.2 2.2 p25 1.5 2.9 2 12 p27 2.7 3.5 4.8 p28 2 p29 2 6 p33 1.6 p35 1.7 6.8 p37 1.7 p62 3 5 Table 3. Identification of canine T cell epitopes from the sequence of fusion protein of CDV. Peptides Kelpie Kelpie Foxhound Foxhound (Dog#125) (Dog#126) P23 3.2 p27 4.5 8.5 p28 1.9 P29 3.6 p33 6 p34 2.1 p35 3.8 10 p36 3 p37 2.5 p38 2.2 P39 2.9 p47 2.7 p62 2.4 p68 2.9 Table 4. Identification of canine T cell epitopes from the sequence of fusion 10 protein of CDV. Peptides Poodle Shitzu Beagle Foxhound# 18 Beagle Foxhound#19 Beagle Foxhound#20 Beagle Foxhound#21 P64 50.0 2.5 2.5 P74 4.0 1.7 6.0 P75 10 2.5 7.2 WO 00/46390 PCT/AU00/00070 15 Once again the same peptides and one additional peptide P32 were tested on cells from additional dogs. These peptides were also shown to react strongly with peripheral blood mononuclear cells from dogs of various breeds immunised with CDV (Table 5), and are therefore identified as strong T-helper 5 epitopes. In conclusion, 26 peptides were identified as canine T helper cell epitopes in the fusion protein of CDV. The sequences of each of these peptides are set out in Table 6. These T helper cell epitopes will have usefulness as components of 10 animal, in particular, canine vaccines, either simply as synthetic peptide based vaccines and as additions to vaccines containing more complex antigens. Table 5. Identification of canine T cell epitopes from the sequence of fusion protein of CDV. 15 Peptides Poodle Shitzu Grey hound Fox Terrier Terrier Cross Kelpie Pointer Border Collie P2 140 <2 <2 <2 . 2.6 2 P4 44 2 <2 2 3.5 2 P6 38 <2 <2 <2 <2 2 P8 100 2 <2 <2 2.8 2 P10 50 2 2.2 2.1 2.4 3 P25 <2 <2 2.6 <2 2.6 <2 P29 2 <2 <2 2 <2 <2 P32 <2 2 <2 <2 <2 <2 P33 <2 <2 <2 <2 2 2 P35 <2 <2 2.2 <2 2 2 P37 <2 <2 <2 2 2 <2 P62 24 <2 <2 <2 <2 <2 P64 50 <2 <2 <2 <2 <2 P68 5 <2 <2 <2 <2 <2 P74 4 <2 <2 <2 <2 <2 P75 10 <2 <2 <2 <2 <2 WO 00/46390 PCT/AUOO/00070 16 Table 6. Sequences of the peptides: P2 SSKTQTHTQQDRPPQPS P4 QPSTELEETRTSRARHS P6 RHSTTSAQRSTHYDPRT P8 PRTSDRPVSYTMNRTRS P10 TRSRKQTSHRLKNIPVH P24 SHQYLVIKLIPNASLIE P22 IGTDNVHYKIMTRPSHQ P23 YKIMTRPSHQYLVIKLI P25 KLIPNASLIENCTKAEL P27 AELGEYEKLLNSVLEPI P28 KLLNSVLEPINQALTLM P29 EPINQALTLMTKNVKPL P32 SGRRQRRFAGWLAGVA P33 FAGWLAGVALGVATAA P34 GVALGVATAAQITAGIA P35 TAAQITAGIALHQSNLN P36 GLALHQSNLNAQAIQSL P37 NLNAQAIQSLRTSLEQS P38 QSLRTSLEQSNKAIEEI P39 EQSNKAIEEIREATQET P47 TELLSIFGPSLRDPISA P62 PRYIATNGYLISNFDES P68 CIRGDTSSCARTLVSGT P64 DESSCVFVSESAICSQN P74 TSTIINQSPDKLLTFIA P75 SPDKLLTFIASDTCPLV Selected sequences of the identified T-cell epitopes were tested for their ability to induce an antibody response to a linked B-cell epitope. Trials were conducted in dogs for assessment of antibody responses. The T-cell epitopes were linked to the B cell epitope LHRH (leuteinising hormone releasing hormone), with the T-cell epitope at the N-terminus and LHRH positioned at the carboxy terminus. WO 00/46390 PCT/AU0O/OOO7O 17 Peptides were synthesised using standard chemistry with Fmoc protection. All peptides were purified to at least 80% purity and the product checked by mass spectroscopy. The peptides were produced as contiguous T-cell - B cell 5 determinants. The LHRH sequence of Pyro Glu -His -Trp - Ser- Tyr- Gly-Leu - Arg - Pro - Gly, or variations of it, was linked to the carboxyl terminus of each respective CDV T- helper epitope. In-vivo evaluation of some of the T-helper epitopes was conducted in two trials, by vaccination of dogs with T-helper - LHRH sequences. 10 EXAMPLE 2. (Trial K9-5) A total of 14 dogs of mixed sex were used in this trial. All had been previously vaccinated with a live CDV vaccine and had also been vaccinated against LHRH. 15 Vaccin e form ulation. Test peptides P25, P27, P35 from CDV were synthesised with LHRH at the C terminus of each T-helper epitope. The LHRH sequence used was the full 10 amino acids of the native LHRH. Each of the vaccine constructs, 20 together with a control peptide comprising a mouse influenza T-cell epitope linked to a repeat malarial B-cell epitope (sequence shown in table below) were purified to -80-90% purity. All peptides were dissolved in 4M urea before dilution with sterile saline to an appropriate volume to give 40nmoles per 1 mL dose. Iscomatrix™ was added to a final concentration of 150ug /1 mL 25 dose as adjuvant together with thiomersal preservative (0.01%). ISCOM™ or Immunostimulating Complex (Barr, Sjolander and Cox, 1998, Advanced Drug Delivery Systems 32: 247 - 271) are a well characterised class of adjuvant comprised of a complex of phospholipid, cholesterol and saponin, usually with a protein incorporated into the complex. Where the 30 complex is formed in the absence of protein antigen, then this complex is termed Iscomatrix™. The saponin used in the preparation of this adjuvant was Quil A. WO 00/46390 PCT/AU00/00070 18 Vaccination, blood samples and assays. All dogs were vaccinated with a lmL dose, delivered in the scruff of the neck. Vaccinations were given at 0 and 4 weeks and venous blood samples were obtained at intervals during the trial. 5 Effective T-cell help was determined by measuring the antibody response to LHRH by ELISA. Biological effectiveness of the peptide based vaccine was determined by measuring the levels of progesterone in female dogs and testosterone in male dogs. 10 Table 7. Trial Groups Peptide Dog Nos. Control -ALNNRFQIKGVELKS ~(NANF)3 104, 998 P25 -LHRH 1-10 70, 73, 127, 993 P27 -LHRH 1-10 20, 94, 101, 105 P35 -LHRH 1-10 19, 96, 100, 102 Results 15 Pre-existing low antibody levels to LHRH were present in all dogs due to immunisation previously with a different vaccine. The control group of dogs exhibited a slow decrease in antibody levels. Dogs immunised with P25-LHRH, P27-LHRH and P35-LHRH all showed strong antibody responses to the B-cell epitope (LHRH). This response 20 persisted to 6 weeks post boost vaccination (see Table 8). The biological potency of the vaccine was demonstrated by a significant reduction in progesterone or testosterone levels (see Tables 9 and 10). WO 00/46390 PCT/AUOO/00070 Table 8 Anti LHRH Titres Anti LHRH Titres Peptide Dog No Prebleeds 2 wks post boost 6wks post boost Control 104 1258 1975 1936 998 2559 1982 1947 Average 1794 1978 1941 Range 1258-2559 1975-1982 1936-1947 P25-LHRH (1-10) 70 856 24245 16697 73 42665 16922 127 1361 21485 19662 993 577 24879 15119 Average 886 23120 17242 Range 0-1361 21485-42665 15119-19662 p27-LHRH (1-10) 20 747 29653 8423 94 41247 22759 101 4256 52724 17353 105 944 12600 8366 Average 2004 25774 12049 Range 747-4256 12600-52724 8366-22759 p35-LHRII (1-10) 19 665 18033 6228 96 1621 26583 5744 100 580 17255 4829 102 180 11740 2963 Average 323 14233 3783 Range 180-1621 11740-26583 2963-6228 WO 00/46390 PCT/AU0O/OOO7O 20 Table 9. Progesterone results (nmol/L) Peptide Dog No. 4wks post primary 2wks post boost 6wks post boost Control 998 5.17 4.28 <0 p25-LHRH (1-10) 127 3.04 4.83 <0 993 1.7 0.87 <0 p27-LIIRII (1-10) 101 0.42 0.14 <0 p35-LIIRII (1-10) 96 31.76 2.15 <0 100 <0 <0 <0 Table 10. Testosterone results (nmol/L) Peptide Dog No. 4wks post primary 2wks post boost 6wks post boost Control 104 9.69 2.51 3.31 p25-LHRH (1-10) 70 <0 <0 <0 73 5.38 <0 <0 p27-LHRH (1-10) 20 1.04 <0 <0 94 3.33 <0 <0 105 >47.7 <0 <0 p35-LIIRH (1-10) 19 4.3 2.77 4.55 102 6.72 <0 <0 The effectiveness of selected T-cell epitopes from the F-protein of CDV in providing T-cell help to elicit antibody responses in dogs proves that the identified sequences are functional. These results also validate the scientific WO 00/46390 PCT/AUOO/00070 21 approach and usefulness of the in vitro screening method for identifying T-helper epitope sequences with in vivo activity. EXAMPLE 3 (Trial K9-8) 5 A total of 35 dogs mixed sex were used in this trial. All had been previously vaccinated with a live CDV vaccine but had not been vaccinated against LHRH. 10 Vaccin e Form ulation: The T-Helper epitopes were linked to a truncated form of LHRH, containing amino acids 2 to 10 of the native 10 amino acid sequence , as shown below: 15 2-10 LHRH His -Trp - Ser- Tyr - Gly - Leu - Arg - Pro - Gly. All vaccines were formulated as for Example 2, ie each 1 mL dose of vaccine contained 40nmoles of peptide, 150|j.g Iscomatrix™, and thiomersal as preservative. 20 Where dogs were vaccinated with a pool of peptides, the concentration of each peptide was adjusted to give equal concentrations and a total amount of 40nmoles of LHRH epitope per 1 mL dose. Vaccination, blood samples and assays. 25 All dogs were vaccinated with a ImL dose, delivered in the scruff of the neck. Vaccinations were given at 0 and 4 weeks and venous blood samples were obtained at intervals during the trial. Effective T-cell help was determined by measuring the antibody response to LHRH by ELISA. Biological effectiveness of the peptide based vaccine was 30 determined by measuring the levels of progesterone in female dogs and testosterone in male dogs. WO 00/46390 PCT/AU00/00070 22 Table 11. Trial Groups Peptide Group Dog Nos. P25-LHRH 2-10 211, 195, 197, 181 P27-LHRH 2-10 203, 191, 186, 201 P35-LHRH 2-10 217, 198, 187, 196 Pool: P25-LHRH 2-10, P27-LHRH 2-10, P35-LHRH 2-10 212, 193, 178, 216, Y3 P2-LHRH 2-10 194, 199, 179, 220 P8-LHRH 2-10 Y4, Y6, 160, 200 P62-LHRH 2-10 219, 185, 221, 177 P75-LHRH 2-10 189, 222, 202, 176 Unvaccinated controls 190, 159 Results 5 Strong antibody responses to LHRH were demonstrated in dogs immunised with the T-cell-LHRH constructs with the T-cell epitopes P25, P27, P35, P62, P75, and the pool of T-cell-LHRH peptides comprising a combination of T-cell epitopes P25, P27 and P35 (see Table 12). Low to undetectable antibody responses were seen in dogs immunised 10 with P2 and P8-LHRH peptides (see Table 12). This was concluded to indicate that these T-cell peptides were not well recognised by Beagle-Foxhound dogs, which is consistent with their identification using PBMCs1 from other dog breeds. The initial screening in Beagle foxhound dogs indicated that this breed of dog does not respond to these 2 T-cell epitopes. 15 As is well understood by those skilled in the art of peptide vaccines the response to individual peptides is genetically determined. The class II Major Histocompatability Complex (MHC II) is polymorphic. Class II molecules at the cell surface function to bind peptides for presentation to T-cells, which is required as part of the activation process for T-cells, including helper T-cells. 20 The allelic forms of MHC class II bind discrete sets of peptide antigens, and thus the response to those antigens is genetically determined. Thus the results are interpreted to indicate that the Beagle - Foxhound breed of dog does not possess the appropriate MHC-II alleles to respond to P2 and P8, but that other WO 00/46390 PCT/AUOO/00070 23 breeds of dog do, eg. the Poodle Shitzu breed that were used to identify these peptides. Control dogs showed no change in antibody levels to LHRH during the trial period and hormone levels were within normal ranges for the age and sex of the dogs (see Table 12). Table 12 Anti-LHRH Titres Anti LHRH Titres Peptide Group Dog No 4 wks after primary 2 wks post boost 4 wks post boost Control 1 159 0 0 0 1 190 0 0 0 GMT Pool 2 Y3 1860 55659 95038 2 178 17900 416036 486793 2 193 8770 211369 189143 2 212 3766 121411 135293 2 216 8378 294769 642293 GMT 6207 177292 237798 P25-LHRH 3 181 1893 152264 131643 3 195 31197 205906 455193 3 197 14423 337698 240543 3 211 20607 142798 131643 GMT 11510 193037 214229 P27-LHRH 4 186 0 11206 17263 4 191 0 59154 125493 4 201 0 17041 34103 4 203 0 1000 857 GMT 0 18523 26698 P35-LHRH 5 187 2009 141775 55797 5 196 4868 237208 158040 5 198 1539 154375 68307 5 217 0 121050 40822 GMT 2469 103085 58002 WO 00/46390 PCT/AU00/00070 24 Table 12 Anti-LHRH Titres (Cont) Anti LHRH Titres Peptide Group Dog No 4 wks after primary 2 wks post boost 4 wks post boost P2-LHRH 6 179 0 0 0 6 194 0 0 0 6 199 0 0 0 6 220 0 0 0 GMT P8-LHRH 7 Y4 0 0 0 7 Y6 0 0 0 7 160 0 1200 ND 7 200 0 8000 2227 GMT P62-LHRH 8 177 1242 3821 2985 8 185 0 146581 67461 8 219 0 29353 28282 8 221 2697 231473 156549 GMT 1830 44167 30728 P75-LHRH 9 176 0 12177 5559 9 189 0 15795 17155 9 202 0 2121 2216 9 222 0 9787 7879 GMT 11201 8746 EXAMPLE 4 5 In vitro T cell Proliferation Assays to demonstrate recognition of Th-epitope incorporated in the peptide vaccines To demonstrate recognition of the Th-epitope within the peptide 10 immunogen PBMCs obtained from dogs immunised with peptide vaccines (dogs from Example 2) were tested against the respective Th-epitopes. The assay was carried out without the enrichment of PBMCs. PBMCs obtained WO 00/46390 PCT/AUOO/00070 25 from Ficoll gradient purification were directly tested against the respective Th-epitope and its truncated versions. The study demonstrated that all the dogs immunised with peptide vaccines responded to the Th-epitope incorporated confirming that T- cell activity resides in the respective 5 sequences (Figures 2-4). Truncated versions of the respective Th-epitopes were also tested to more closely define the T-cell activity within the sequences. It was observed that for P25 the full sequence of 17 residues was better than the shorter peptides of 15 and 12 residues, each truncated from the N-terminus of the sequence (Figure 2). This implies that the T-cell activity is 10 towards the N-terminus or middle of the 17-residue peptide. A similar observation was made with P27, the 17 residue long peptide was a better simulator than the 15-mer truncated from the N-terminus (Figure 3). This observation again suggested that the T-cell activity may reside towards the middle or the N-terminus of the full length peptide. 15 In the case of P35 and its shorter versions, except for one dog (#102), the other three dogs responded as well to the 12 residue peptide as to the full length 17 residue one (Figure 4). In dog # 102 the 15 residue peptide was more stimulatory than the full length peptide. From this it can be deduced that that the first two residues in the sequence of P35 may not be essential and 20 that the activity is towards the middle or C-terminus of the peptide. EXAMPLE 5 Trial in BALB/c mice 25 The canine vaccines with CDV-F derived Th-epitopes and LHRH used in Example 3 were also used to immunise BALB/c mice to investigate if the Th-epitopes would be functional in a different animal species. Vaccine Formulation 30 All vaccines were formulated as for Example 3 except that they were diluted further so that 100(j.l doses contained 2.7 nmoles of peptide and 10^g of Iscomatrix™ and thiomersol as preservative. Vaccination, blood samples and assays. 35 Mice were vaccinated with 100p,l of the vaccine at the base of tail. Vaccinations were given at 0 and 4 weeks and animals bled at intervals after WO 00/46390 PCT/AUOO/00070 26 each vaccination from the retro-orbital plexus. Effective T-cell help was determined by measuring the antibody response to LHRH by ELISA. Results 5 Mice immunised with P25-LHRH and pool of peptides comprising of P25-LHRH, P27-LHRH and P35-LHRH generated high antibody titres to LHRH. Peptides P35 and P75 generated low antibody titres whereas mice immunised P2, P8 and P62 had undetectable levels of anti-LHRH antibodies (Table 13). 10 It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in the specific embodiments without departing from the spirit or scope of the invention as broadly described. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive. 15 • # * Table 13. Anti-LHRH antibody titres in mice immunised with CDV -F derived T cell epitope-LHRH vaccines ® O Groups 4 weeks post first vaccination 2 weeks post second vaccination Mouse 1 Mouse 2 Mouse 3 Mouse 4 Mouse 5 Mouse 1 Mouse 2 Mouse 3 Mouse 4 Mouse 5 Group l(control) <100 <100 <100 <100 Group 2 (pool) 100 126 200 126 200 16,000 16,000 16,000 16,000 16,000 Group 3 (p25-LHRH) 126 400 282 100 282 16,000 16,000 16,000 16,000 16,000 Group 5 (P35-LHRH) <100 <100 <100 <100 <100 1,412 800 <100 <100 <100 Group 6 (P2-LHRH) <100 <100 <100 <100 Group 7 (P8-LHRH <100 <100 <100 <100 <100 <100 <100 <100 Group 8 (p62-LHRH <100 <100 <100 126 126 <100 Group 9 (p75-LHRH <100 <100 <100 <100 <100 <100 <100 316 3,162 <100 </div>

Claims

<div class="application article clearfix printTableText" id="claims"> 5^ II L 28 THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS:

1. AT helper cell epitope, the epitope being contained within a peptide sequence selected from the group consisting of SSKTQTHTQQDRPPQPS (SEQ ID NO: 1) 5 QPSTELEETRTSRARHS (SEQ ID NO: 2): RHSTTSAQRSTHYDPRT (SEQ ID NO: 3) PRTSDRPVSYTMNRTRS (SEQ ID NO: 4); TRSRKQTSHRLKNIPVH (SEQ ID NO: 5) SHQYLVIKLIPNASLIE (SEQ ID NO: 6); IGTDNVHYKIMTRPSHQ (SEQ ID NO: 6) YKIMTRPSI-IQYLVHCLI (SEQ ID NO: 8); KLIPNASLIENCTKAEL (SEQ ID NO: 9) AELGEYEKLLNSVLEPI (SEQ ID NO: 10); KLLNSVLEPINQALTLM (SEQ ID NO 10 11); EPINQALTLMTKNVKPL (SEQ ID NO: 12); FAGWLAGVALGVATAA (SEQ ID NO: 13); GVALGVATAAQITAGIA (SEQ ID NO: 14): TAAQITAGIALHQSNLN (SEQ ID NO: 15); GIALHQSNLNAQAIQSL (SEQ ID NO: 16); NLNAQAIQSLRTSLEQS (SEQ ID NO: 17); QSLRTSLEQSNKAIEEI (SEQ ID NO: 18); EQSNKAIEEIREATQET (SEQ ED NO: 19); TELLSIFGPSLRDPISA (SEQ ID NO: 20); PRYIATNGYLISNFDES 15 (SEQ ID NO: 21); CIRGDTSSCARTLVSGT (SEQ ID NO: 22); DESSCVFVSESAICSQN (SEQ ID NO: 23); TSTIINQSPDKLLTFIA (SEQ ID NO: 24), SPDKLLTFIASDTCPLV (SEQ ID NO: 25) and SGRRQRRFAGWLAGVA (SEQ ID NO: 26). 20

2. A composition for use in raising an immune response in an animal, the composition comprising at least one T helper cell epitope, the at least one T helper cell epitope being contained within a peptide sequence selected from the group consisting of SSKTQTHTQQDRPPQPS (SEQ ID NO: 1); QPSTELEETRTSRARHS (SEQ ID NO 2): RHSTTSAQRSTHYDPRT (SEQ ID NO: 3); PRTSDRPVSYTMNRTRS (SEQ ID NO 25 4); TRSRKQTSHRLKNIPVH (SEQ ID NO: 5); SHQYLVIKLIPNASLIE (SEQ ID NO 6); IGTDNVHYKIMTRPSHQ (SEQ ID NO: 6); YKIMTRPSI-IQYLVIKLI (SEQ ID NO 8); KLIPNASLIENCTKAEL (SEQ ID NO: 9); AELGEYEKLLNSVLEPI (SEQ ID NO 10); KLLNSVLEPINQALTLM (SEQ ID NO: 11); EPINQALTLMTKNVKPL (SEQ ID NO: 12); FAGWLAGVALGVATAA (SEQ ID NO: 13); GVALGVATAAQITAGIA 30 (SEQ ID NO: 14): TAAQITAGIALHQSNLN (SEQ ID NO. 15) GIALHQSNLNAQAIQSL (SEQ ID NO: 16); NLNAQAIQSLRTSLEQS (SEQ ID NO 17); QSLRTSLEQSNKAIEEI (SEQ ID NO: 18); EQSNKAIEEIREATQET (SEQ ID NO Inte.lsciuaf Prcpsrty Office of NZ \\fbrm-fp\windocs$\pxm\specification\94088cmpmro.doc 2oJUN 2003 RECFIVcn 51 Q ^ © £ 29 19); TELLSIFGPSLRDPISA (SEQ ID NO: 20); PRYIATNGYLISNFDES (SEQ ID NO: 21); CIRGDTSSCARTLVSGT (SEQ ID NO: 22); DESSCVFVSESAICSQN (SEQ ID NO: 23); TSTIINQSPDKLLTFIA (SEQ ID NO: 24), SPDKLLTFIASDTCPLV (SEQ ID NO: 25) and SGRRQRRFAGWLAGVA (SEQ ID NO: 26). 5

3. A composition as claimed in claim 2 in which the composition comprises at least one peptide selected from the group consisting of SSKTQTHTQQDRPPQPS (SEQ ID NO: 1); QPSTELEETRTSRARHS (SEQ ID NO: 2): RHSTTSAQRSTHYDPRT (SEQ ID NO: 3); PRTSDRPVSYTMNRTRS (SEQ ID NO: 4); TRSRKQTSHRLKNIPVH (SEQ ID 10 NO: 5); SHQYLVIKLIPNASLIE (SEQ ID NO: 6); IGTDNVHYKIMTRPSHQ (SEQ ID NO: 6); YKIMTRPSI-IQYLVIKLI (SEQ ID NO: 8); KLIPNASLIENCTKAEL (SEQ ID NO: 9); AELGEYEKLLNSVLEPI (SEQ ID NO: 10); KLLNSVLEPINQALTLM (SEQ ID NO: 11); EPINQALTLMTKNVKPL (SEQ ID NO: 12); FAGWLAGVALGVATAA (SEQ ID NO: 13); GVALGVATAAQITAGIA (SEQ ID NO: 14) 15 TAAQITAGIALHQSNLN (SEQ ID NO: 15); GIALHQSNLNAQAIQSL (SEQ ID NO 16); NLNAQAIQSLRTSLEQS (SEQ ID NO: 17); QSLRTSLEQSNKAIEEI (SEQ ID NO 18); EQSNKAIEEIREATQET (SEQ ID NO: 19); TELLSIFGPSLRDPISA (SEQ ID NO 20); PRYIATNGYLISNFDES (SEQ ED NO: 21); CIRGDTSSCARTLVSGT (SEQ ID NO 22); DESSCVFVSESAICSQN (SEQ ID NO: 23); TSTIINQSPDKLLTFIA (SEQ ID NO 20 24), SPDKLLTFIASDTCPLV (SEQ ID NO: 25) and SGRRQRRFAGWLAGVA (SEQ ID NO: 26).

4. A composition as claimed in claim 2 or claim 3 in which the composition further comprises at least one B cell epitope and/or at least one CTL epitope. 25

5. A composition as claimed in claim 4 in which the at least one B cell epitope and,/or the at least one CTL Ppitope are linked to at least one of the T helper cell epitopes. 30

6. A composition as claimed in claim 5 in which the composition comprises a plurality of epitope constructs in which each conjugate comprises at least one T helper cell epitope and at least one B cell epitope. Intei'sctua! Property Office of NZ 2 o JUN 2003 \\fbrm-fp\windocs$\pxm\specification\94088cmpmro.doc RECEIVED 30

7. A composition as claimed in claim 5 in which the composition comprises a plurality of epitope constructs in which each conjugate comprises at least one T helper cell epitope and at least one CTL epitope. 5

8. A composition as claimed in any one of claims 4 to 7 in which the composition comprises an LHRH B cell epitope.

9. A composition as claimed in claim 2 in which the composition comprises a plurality of T helper cell epitopes. 10

10. A composition as claimed in claim 9 in which the plurality of T cell epitopes is a single polypeptide.

11. A composition as claimed in claim 9 or claim 10 in which the composition further 15 comprises at least one B cell epitope and/or at least one CTL epitope.

12. A composition as claimed in claim 11 in which the least one B cell epitope and/or at least one CTL epitope is linked to the plurality of T helper cell epitopes. 20

13. A composition as claimed in claim 11 or claim 12 in which the composition comprises an LHRH B cell epitope.

14. A composition as claimed in any one of claims 2 to 13 in which the composition comprises an adjuvant. 25

15. A composition as claimed in claiml4 in which the adjuvant comprises ISCOMs or Iscomatrix.

16. Use of a T Helper cell epitope as defined in claim 1 in the preparation of a 30 medicament for inducing an immune response in an animal. Intellectual Property \\fbrin-fp\windocs$\pxm\specifi cation\94088cmpmro.doc Office of Nz 2 o JUN 2003 Rece/veD 31 51 • " 15 20 25

17. Use of the composition as claimed in any one of claims 2 to 15 in the preparation of a medicament for inducing an immune response in an animal.

18. A composition for use in raising an immune response in an animal, the composition comprising two or more T helper cell epitopes, the T helper cell epitopes being contained within a peptide sequence selected from the group consisting of KLIPNASLIENCTKAEL (SEQ ID NO: 9), AELGEYEKLLNSVLEPI (SEQ ID NO: 10), and TAAQITAGIALHQSNLN (SEQ ID NO: 15).

19. The composition of claim 18, wherein the T helper cell epitopes are contained within the peptide sequences KLIPNASLIENCTKAEL (SEQ ID NO: 9), and AELGEYEKLLNSVLEPI (SEQ ID NO: 10).

20. The composition of claim 18, wherein the T helper cell epitopes are contained within the peptide sequences KLIPNASLIENCTKAEL (SEQ ID NO: 9) and TAAQITAGIALHQSNLN (SEQ ID NO: 15).

21. The composition of claim 18, wherein the T helper cell epitopes are contained within the peptide sequences AELGEYEKLLNSVLEPI (SEQ ID NO: 10) and TAAQITAGIALHQSNLN (SEQ ID NO: 15).

22. The composition of claim 18, wherein the T helper cell epitopes are contained within the peptide sequences KLIPNASLIENCTKAEL (SEQ ID NO: 9), AELGEYEKLLNSVLEPI (SEQ ID NO: 10) and TAAQITAGIALHQSNLN (SEQ ID NO: 15).

23. Use of a composition as defined in any one of claims 18 to 22 in the preparation of a medicament for inducing an immune response in an animal.

24. The T helper cell epitope according to claim 1 substantially as described herein with reference to any example thereof. 2 o JUN 2003 \\fbrm-fp\windocs$\pxm\specification\94088cmpmro.doc Received 513482 32

25. A composition for use in raising an immune response in an animal according to any one of claims 2 to 15 or 18 to 22 as described herein with reference to any example thereof. 5

26. The use of a T helper cell epitope according to claim 16 as described herein with reference to any example thereof.

27. The use of a composition according to claim 17 or claim 23 as described herein with reference to any example thereof. 10 Dated this eleventh day of June 2003 15 The University of Melbourne, CSL Limited, Commonwealth Scientific and Industrial Research Organisation, The Council of the Queensland Institute of Medical Research, Walter and Eliza Hall Institute of Medical Research Patent Attorneys for the Applicant: 20 F B RICE & CO 2 o JUN 2003 Wfbrm-fp\windocsS\pxm\specification\94088cmpmro.doc </div>